Bagheri Abouzar, Khorram Khorshid Hamid Reza, Mowla Seyed Javad, Mohebbi Hassan Ali, Mohammadian Azam, Yaseri Mehdi, Solaymani-Dodaran Masoud, Sherafatian Masih, Tavallaie Mahmood
Genetic Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Avicenna J Med Biotechnol. 2017 Oct-Dec;9(4):189-195.
Diagnosis of Non-small Cell Lung Cancer (NSCLC) at an early stage is a daunting challenge due to the deficiency of specific noninvasive markers. MicroRNAs (miRNAs) play important roles in the initiation and progression of NSCLC. Measuring miRNA expression levels could provide a potential approach for the diagnosis of NSCLC. Our goals were to examine miR-223, miR-212, miR-192, miR-3074, SNORD33 and SNORD37 expression levels in tissue and sputum of NSCLC patients and cancer free subjects for molecular diagnosis of NSCLC.
Relative expressions of miR-223, miR-212, miR-192, miR-3074, SNORD33 and SNORD37 were examined with quantitative real-time RT-PCR assay in tissue and sputum obtained from 17 NSCLC patients and 17 controls.
miR-3074 was upregulated in tissue samples of NSCLC patients compared with control group. miR-223 was upregulated, miR-212 and SNORD37 were downergulated in sputum samples of patients compared with controls. miR-223 quantification produced 82% sensitivity and 95% specificity with areas under the ROC curve at 0.90 in detection of NSCLC.
miR-223 clearly discriminated cancer patients from cancer-free subjects and our results suggest that miR-223 could be a diagnostic useful biomarker. The measurement of altered miRNA expression in sputum samples manifested the potential noninvasive approach for detection of lung cancer.
由于缺乏特异性非侵入性标志物,早期诊断非小细胞肺癌(NSCLC)是一项艰巨的挑战。微小RNA(miRNA)在NSCLC的发生和发展中起重要作用。检测miRNA表达水平可为NSCLC的诊断提供一种潜在方法。我们的目标是检测NSCLC患者和无癌受试者的组织及痰液中miR-223、miR-212、miR-192、miR-3074、SNORD33和SNORD37的表达水平,以用于NSCLC的分子诊断。
采用定量实时RT-PCR法检测从17例NSCLC患者和17例对照者获取的组织及痰液中miR-223、miR-212、miR-192、miR-3074、SNORD33和SNORD37的相对表达。
与对照组相比,NSCLC患者组织样本中miR-3074上调。与对照组相比,患者痰液样本中miR-223上调,miR-212和SNORD37下调。在检测NSCLC时,miR-223定量分析的灵敏度为82%,特异性为95%,ROC曲线下面积为0.90。
miR-223能明显区分癌症患者和无癌受试者,我们的结果表明miR-223可能是一种有用的诊断生物标志物。检测痰液样本中miRNA表达的改变显示了检测肺癌的潜在非侵入性方法。